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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928500Generated: November 1, 2026

3-(tert-Butylaminosulphonyl)benzeneboronic acid → HCID 57469120, compound

https://huagongshe.com/reaction/1928500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(tert-Butylaminosulphonyl)benzeneboronic acidHCID 44119538—
ReactantHCID 57468751HCID 57468751—
ProductHCID 57469120HCID 57469120—

Reaction Steps

N-tert-Butyl-3-{4-[6-(3-ethoxy-4-trifluoromethyl-phenyl)-4-trifluoromethyl-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonamide was prepared from 2-(2-chloro-pyridin-4-yl)-6-(3-ethoxy-4-trifluoromethyl-phenyl)-4-trifluoromethyl-pyrimidine (example E.108) (0.185 g, 0.41 mmol) and commercially available 3-(tert.-butylsulfamoyl)-phenylboronic acid (0.13 g, 0.50 mmol) according to the general procedure VI. Obtained as an off-white solid (0.24 g), which was subsequently deprotected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-e8b0f75a9aa44748b6c1474e9faddb97
Source noteuspto-grants-2012_05